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Azidoethyl-SS-ethylazide

  CAS No.: 352305-38-5   Cat No.: BADC-01118   Purity: >99.3% 4.5  

Azidoethyl-SS-ethylazide is a bifunctional cleavable ADC linker featuring azide and disulfide groups, enabling bioorthogonal conjugation and redox-sensitive drug release in targeted therapeutics.

Azidoethyl-SS-ethylazide

Structure of 352305-38-5

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Category
ADC Linker
Molecular Formula
C4H8N6S2
Molecular Weight
204.28
Shipping
Room temperature
Shipping
-20°C

* For research and manufacturing use only. We do not sell to patients.

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Synonyms
1,2-bis(2-azidoethyl)disulfane; bis(2-azidoethyl) disulfide; 1,6-Diazido-3,4-dithiahexane; 1-azido-2-(2-azidoethyldisulfanyl)ethane
IUPAC Name
Canonical SMILES
C(CSSCCN=[N+]=[N-])N=[N+]=[N-]
InChI
InChI=1S/C4H8N6S2/c5-9-7-1-3-11-12-4-2-8-10-6/h1-4H2
InChIKey
SYKSDZXTWAVSIP-UHFFFAOYSA-N
Solubility
10 mm in DMSO
Appearance
Solid
Shelf Life
0-4°C for short term (days to weeks), or -20°C for long term (months).
Shipping
Room temperature
Storage
-20°C
Form
Solid

Azidoethyl-SS-ethylazide, a versatile bifunctional cross-linker, plays a significant role in chemical biology and biochemistry. Here are four key applications of Azidoethyl-SS-ethylazide, presented with high perplexity and burstiness:

Protein-Protein Interaction Studies: Widely utilized in research, Azidoethyl-SS-ethylazide facilitates the investigation of protein-protein interactions by cross-linking interacting proteins. This cross-linker, when photoactivated, triggers the formation of covalent bonds between proximal proteins. The resulting stable complexes are subject to analysis using advanced techniques like mass spectrometry, allowing researchers to pinpoint binding partners and interaction sites with precision.

Drug Delivery Systems: In the realm of drug delivery, Azidoethyl-SS-ethylazide is a valuable tool for designing targeted systems. By linking therapeutic agents to biomolecules via azido groups, researchers create prodrugs that release active compounds selectively at predetermined sites in the body. This strategic approach not only boosts drug efficacy but also minimizes off-target effects, ensuring efficient delivery to diseased tissues while enhancing patient outcomes.

Bioorthogonal Chemistry: Within the realm of bioorthogonal chemistry, Azidoethyl-SS-ethylazide serves as a versatile reagent for labeling biomolecules in live cells. Its azide groups participate in a strain-promoted azide-alkyne cycloaddition (SPAAC) reaction with complementary alkyne or cyclooctyne groups, enabling the specific tagging of proteins, nucleic acids, or lipids without perturbing cellular processes. This innovative technique facilitates imaging and tracking studies, expanding our understanding of cellular dynamics.

Material Science: Azidoethyl-SS-ethylazide finds application in the creation of advanced materials with unique properties. By incorporating azido groups into polymers, researchers can craft cross-linked networks and hydrogels with heightened mechanical strength and stability. These tailor-made materials hold promise in diverse fields such as tissue engineering, where they provide crucial support for cell growth and integration within the tissue matrix.

The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

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Historical Records: Azido-C2-SS-PEG2-C2-acid | Propargyl-PEG1-SS-PEG1-PFP ester | Propargyl-PEG1-SS-PEG1-propargyl | Hydroxy-PEG3-SS-PEG3-alcohol | Propargyl-PEG1-SS-PEG1-acid | Acid-PEG3-SS-PEG3-acid | Propargyl-PEG1-SS-alcohol | Alkyne-SS-COOH | NHS-SS-Ph | Bis-(PEG6-acid)-SS | Azidoethyl-SS-ethylazide
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